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HS Code |
649921 |
| Product Name | 3-(Bromomethyl)Quinoxalin-2(1H)-One |
| Cas Number | 918792-58-2 |
| Molecular Formula | C9H7BrN2O |
| Molecular Weight | 239.07 g/mol |
| Appearance | Light yellow to brown solid |
| Melting Point | 140-144°C |
| Purity | Typically ≥98% |
| Solubility | Soluble in DMSO and DMF |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
As an accredited 3-(Bromomethyl)Quinoxalin-2(1H)-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 5g amber glass bottle with tamper-evident seal, labeled “3-(Bromomethyl)Quinoxalin-2(1H)-One,” including hazard pictograms and CAS number. |
| Shipping | 3-(Bromomethyl)Quinoxalin-2(1H)-One should be shipped in tightly sealed containers, protected from moisture and light. It must be packaged according to hazardous material regulations and transported at room temperature. Appropriate hazard labeling and documentation are required to ensure safe handling and compliance with local and international shipping standards for chemicals. |
| Storage | 3-(Bromomethyl)Quinoxalin-2(1H)-one should be stored in a tightly sealed container, protected from light and moisture. Keep the chemical in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Ensure clear labeling and restrict access to trained personnel. Use appropriate personal protective equipment when handling or transferring the compound. |
Applications of 3-(Bromomethyl)Quinoxalin-2(1H)-One in Industrial Manufacturing3-(Bromomethyl)Quinoxalin-2(1H)-One serves as a specialty intermediate in various advanced chemical sectors. Through controlled synthesis, strict adherence to downstream quality protocols, and responsive adjustment to end-user specifications, this intermediate plays critical roles in regulated industrial supply chains. Below are several focused applications, each reflecting practical, real-world industrial usage supported by distinct compliance, formulation, and operational frameworks. 1. Pharmaceutical Intermediate for CNS Active Compound SynthesisPharmaceutical process engineers utilize 3-(Bromomethyl)Quinoxalin-2(1H)-One in the multi-step synthesis of quinoxaline-based central nervous system (CNS) drug candidates. Reaction optimization is governed by stringent specifications on impurity profiles and enantiomeric excess. In industrial campaigns, operators monitor bromination selectivity and downstream integration to minimize cross-contamination and batch rejection. Batch documentation and traceability support compliance in both kilo lab and commercial-scale setups. Industry compliance standards
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2. Precursor for Specialty Agrochemical Actives (Herbicides, Fungicides)Agrochemical formulators employ this compound as a critical building block in the assembly of systemic quinoxaline-based herbicides and fungicides. Process optimization considers both thermal degradation limits and required substitution patterns for specific biological targets. Mixing protocols emphasize control of residual bromide species to avoid phytotoxicity. Integration into continuous or semi-continuous agrochemical lines mandates strict documentation and in-process release criteria. Industry compliance standards
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3. Intermediate for Advanced Dye and Pigment SynthesisDye manufacturers incorporate 3-(Bromomethyl)Quinoxalin-2(1H)-One as a key precursor in the design of lightfast, solvent-resistant heterocycle dyes for technical textiles and coatings. The focus lies on sharp color control and enhanced wash-fastness required by industrial textile finishing lines. Operators maintain strict batch-to-batch reproducibility, and surface activation steps are closely monitored to improve integration with polymer matrices. Industry compliance standards
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4. Intermediate for Molecular Sensor and Analytical Reagent ProductionProducers of analytical diagnostics use this molecule for the synthesis of responsive quinoxaline-based fluorescent probes. The necessary purity profile demands strict control of ionic impurities due to end-use in trace-level analytical assays. Manufacturing maintains segregation from general-purpose production to ensure compliance with analytical reagent reference standards, and technical documentation aligns with end-user assay protocols. Industry compliance standards
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Everyone in the industry knows that the search for specialized chemical intermediates has grown only more intense over the last decade. From where we stand as the team crafting 3-(Bromomethyl)Quinoxalin-2(1H)-One, we see firsthand the demand for precise, consistent calendared batches. Our production team handles every step of the bromination, kinetic controls, and crystallization, not in theory, but among the hum of reactors, with real eyes on the reaction flask. Years of working the specifics—right solvent choice, heating profiles, temperature windows, in-line monitoring—have taught us that reliable supply depends on more than simple compliance; it requires the kind of loyalty to detail that comes only from producing ton after ton of a single specialty compound.
3-(Bromomethyl)Quinoxalin-2(1H)-One (CAS: 872-33-9) is not simply a raw material; most of its value appears downstream, enabling manufacturers in pharmaceuticals and specialty materials to link up heterocycles and create active compounds that shape new therapies. The crystalline solid we deliver comes standard in 99% purity, though our lot records show that recent batches have consistently achieved even tighter spec due to advances in our drying and purification lines. We package as per project needs: double-lined bags for drumful quantities, smaller containers for pilot runs, and custom weights calibrated for direct transfer into synthesis.
Our chemists involved in synthesis projects confirm time and again how much smoother the process flows with a clean, well-processed intermediate. No one likes extra work at the purification step, especially when troubleshooting means halting a production line. Granular, non-clumping material, uniform particle size: these details might look simple on paper, but on a hot summer day in the plant, the difference between easy transfer and a stuck hopper spells an hour lost—or gained—in a twelve-hour shift. Many suppliers cut corners juggling multiple product lines, recycling solvents, and cross-contaminating sensitive brominated intermediates with persistent organic residues. Over the years, we’ve poured resources into separated production spaces for halogenation and tailored washing sequences to keep cross-reactivity below detection limits. That’s an investment that pays off not in marketing copy, but in the near-zero complaint rate from large buyers who can’t afford unpredictable crystallization or side-product formation later in their chain.
Our experience tells us the main users of 3-(Bromomethyl)Quinoxalin-2(1H)-One are often in the research labs of pharma and specialty chemicals, working up the backbone of novel molecules. They deal with the stubborn reactivity of aromatic bromides, the fine balance between nucleophilicity and selectivity in coupling reactions, and the ever-present high bar for purity in regulated environments. Nucleophilic substitution at the bromomethyl position lets R&D chemists test out a range of linkers or side chains, while preserving the quinoxalinone core that shows up in kinase inhibitors or CNS-active scaffolds. A minor fluctuation in water content, a trace level of residual solvent, or unexpected isomeric contaminants makes a huge difference at scale for downstream reactions. Years of hands-on analysis in our facility have shown that regular attention to line flushing, live Karl Fischer readings, and in-process chromatography can make these headaches disappear before a single drum leaves the loading ramp.
Some customers used to report batch-to-batch inconsistency from generalist suppliers, with textures ranging from stubbornly sticky to excessively powdery. Operators hate spending extra time weighing out lumps or dealing with airborne fines clogging up their containment systems. By modifying our crystallization window and post-drying sieving, we’ve stabilized not only purity but also the physical form, so what you get is what you expect: free-flowing, easy to handle, and easy to dose reliably into your own reactors. Working closely with frontline users, we’ve dropped the guesswork out of process development for the API and intermediate houses that rely on our products.
Many practitioners in chemical synthesis get frustrated when small supply issues mushroom into lost days on high-value campaigns. Over years of site audits and customer visits, we heard about the “small things” that cause these stoppages: inclusions of colored byproducts, off-odors from partial oxidations, mysterious spikes in halide readings. Shifting from generic channel supplies to in-house manufacture, with deep vertical integration, gave us control over not just which chemistries we run but the quality of every input and step along the way. In practice, that means more than just strong batch records. We build our own process analytics, test every incoming lot of starting materials ourselves, and recalibrate reactors at the end of every month.
On the macro scale, the market shifts fast—a few years back, demand for this bromomethyl quinoxalinone shot up as more drug discovery programs turned to heterocycle-rich scaffolds. At the same time, environmental scrutiny got stricter, especially for halogenated intermediates. We invested early in closed-loop bromine recovery systems, which not only keep emissions in check but cut our costs in the long run. Soil and water monitoring at our production site is routine, supporting the growing demand among our customers for both “green” sourcing and full traceability. These aren’t marketing terms for us—they’re operational standards we measure quarterly, and produce certified documentation for each production lot.
Chemists shopping for 3-(Bromomethyl)Quinoxalin-2(1H)-One have options, but not all sources meet the same demands. In lab-scale syntheses, small differences in impurity levels or unwanted halide content may be absorbed by later purification. Powerful chromatography equipment can clean up a dirty feedstock—at a cost. In full-scale operations, residual bromides or hydrolyzed material can wreak havoc. Failed runs and discarded kilo-quantities cost many times more than paying a slight premium for top-grade intermediate straight from an experienced maker. Customers large and small have told us that consistency, traceability, and technical support influence reorder decisions far more than marginal price swings between suppliers.
Beyond just purity, the difference comes in technical support and supply reliability. Substitution reactions, particularly those targeting the methylene group, respond poorly to batch variation caused by ambient moisture or incomplete conversion during bromination. Over the years, we have optimized drying cycles and introduced gas-tight handling for outgoing shipments, extending shelf life and protecting sensitive functionality until the compound hits the customer’s bench. Raw analytical data—NMR, LC-MS, elemental analysis—accompanies each shipment, satisfying both regulatory filings and in-house QC labs. Feedback from process chemists regularly comes back to us, driving further round-by-round improvements in both process and customer service.
3-(Bromomethyl)Quinoxalin-2(1H)-One belongs on the shelf in a well-run, tightly controlled setting. As a halogenated intermediate, it demands respect from both the handling and regulatory side. From day one, our crews treat dust, skin, and fume exposure as site-level priorities, with continuous extraction, regular monitoring, and clear SOPs that have been stress-tested in batch after batch. Our development chemists have spent late nights at the pilot plant, troubleshooting filtration blockages and maximizing yield while keeping levels of potentially harmful side products far below established exposure limits. Regular audits of our air and effluent controls are more than just box-ticking—they’re woven into the structure of our operational DNA.
Any operation focusing on scale knows that solvents and reagents play a huge role in both the economics and the sustainability of halogenated intermediates. In redesigning our production process to minimize waste and streamline downstream separation, we chose greener, recyclable solvents. Old habits led most industry players to default halocarbon washings and heavy-metal scavengers; continuous improvement has taken us beyond short-term expedience to proven, low-impact alternatives. Consistent engagement with local regulatory authorities, detailed waste manifests, and open-book records mean we walk the talk—not because external audits require it, but because decades in this sector reveal that shortcuts in waste management always find their way back to haunt the plant and the people running it.
The use cases for our quinoxalinone derivative cluster heavily in advanced research and late-stage development. Project managers have come to us for pilot quantities during early process scouting, returning years later for multi-ton requirements as pipelines advance toward scale-up and registration batches. Our role extends beyond shipping pure material: supporting method development, sharing insight on crystallization or cleaning routines, and providing targeted documentation. Whether it’s a clinical-stage startup or a multinational scaling up an in-licensed synthesis route, our access to every lot record, analytical dataset, and run parameter gives them confidence to move from kilo to ton, making their own scale-up practical and predictable.
Among our strongest clients, best practices trickle down: clear labeling, batch-specific technical reports, and open lines to production chemists. If a specific impurity rears its head in a downstream transformation, our team jumps in, tracing back through archived production data to pinpoint and resolve the cause. We treat every complaint and every compliment as direct feedback that shapes tomorrow’s process. Our proximity to customer application teams gives us real-world intelligence on which side-reactions cause the biggest headaches, helping us further tighten our process windows, drying curves, and batch release controls.
Decades of experience with heterocyclic chemistry have taught us that customer needs never remain static. R&D requirements continue to evolve, more stringent sustainability metrics loom, and even stricter regulatory thresholds seem certain. Every year brings news of a new application, a new substitution route, or a demand for more documentation, shorter lead times, or sustainable sourcing. Our response is to keep R&D and production teams working side by side, turning practical issues into concrete process improvements. Whether it’s more energy-efficient bromination cycles, live on-site analytics, or more durable, traceable packaging, we address each challenge backed by years of hands-on chemical manufacturing.
Some of our proudest achievements come not just from mass-producing a standard intermediate, but from innovating alongside end-users—modifying particle size, eliminating a trace impurity, customizing lot sizes, or expediting shipments in response to real research deadlines. The expectation is always moving and so are our internal targets. Every process change, every quality control tweak, comes down to one question: does this make life easier for the chemists and engineers who rely on our 3-(Bromomethyl)Quinoxalin-2(1H)-One? If not, it’s back to the pilot line.
In this space, only manufacturers who personally stand behind every drum, every batch, have the perspective needed to balance efficiency, compliance, and long-term partnerships. 3-(Bromomethyl)Quinoxalin-2(1H)-One may not make the headlines, but for anyone crafting complex molecules at scale, it is often the difference between success and unplanned troubleshooting. Each batch shipped reflects our day-to-day dedication—the kind that comes not from theory, but from the experience of real chemical manufacturing.